Variant report

Variant	rs73450959
Chromosome Location	chr15:77900146-77900147
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:77891327..77896574-chr15:77898422..77902980,9	K562	blood:
2	chr15:77898597..77902901-chr15:77907031..77910421,4	K562	blood:
3	chr15:77899584..77901870-chr15:77910990..77913716,3	K562	blood:
4	chr15:77899424..77903075-chr15:77914224..77917029,3	K562	blood:
5	chr15:77888337..77891310-chr15:77900138..77902706,2	MCF-7	breast:
6	chr15:77894564..77896146-chr15:77898435..77900182,2	K562	blood:

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs11853548	1.00[EUR][1000 genomes]
rs11853824	1.00[EUR][1000 genomes]
rs11854532	1.00[EUR][1000 genomes]
rs11855576	1.00[EUR][1000 genomes]
rs11857529	1.00[EUR][1000 genomes]
rs12324340	1.00[EUR][1000 genomes]
rs2667765	1.00[EUR][1000 genomes]
rs28439897	1.00[EUR][1000 genomes]
rs28498563	1.00[EUR][1000 genomes]
rs28498879	1.00[EUR][1000 genomes]
rs28557414	1.00[EUR][1000 genomes]
rs28634734	1.00[EUR][1000 genomes]
rs28635388	1.00[EUR][1000 genomes]
rs34611551	1.00[EUR][1000 genomes]
rs57215429	1.00[EUR][1000 genomes]
rs57365401	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57738968	1.00[EUR][1000 genomes]
rs58372659	1.00[EUR][1000 genomes]
rs58432220	1.00[EUR][1000 genomes]
rs58490956	1.00[EUR][1000 genomes]
rs58723442	1.00[EUR][1000 genomes]
rs58745170	1.00[EUR][1000 genomes]
rs59320137	1.00[EUR][1000 genomes]
rs60322323	1.00[EUR][1000 genomes]
rs60380768	1.00[EUR][1000 genomes]
rs60772286	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60934296	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6495243	1.00[EUR][1000 genomes]
rs7181139	1.00[EUR][1000 genomes]
rs7182984	1.00[EUR][1000 genomes]
rs73448973	1.00[EUR][1000 genomes]
rs73450724	1.00[EUR][1000 genomes]
rs74025393	1.00[EUR][1000 genomes]
rs8037835	1.00[EUR][1000 genomes]
rs8038325	1.00[EUR][1000 genomes]
rs907375	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs907394	1.00[EUR][1000 genomes]
rs907397	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040852	chr15:77160237-78137541	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv916323	chr15:77485765-78121259	Enhancers Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv833060	chr15:77816654-78035204	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	esv1806097	chr15:77817889-78301377	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
5	nsv904415	chr15:77845959-77943935	Weak transcription Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv904416	chr15:77845959-77967416	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv904417	chr15:77851535-77935992	Weak transcription Flanking Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv904418	chr15:77851535-77963887	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv1036749	chr15:77884026-77912408	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv904419	chr15:77897197-77943935	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77895800-77901200	Enhancers	Fetal Muscle Leg	muscle
2	chr15:77896200-77900400	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr15:77896200-77900600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr15:77896400-77900200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr15:77896600-77901400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr15:77896800-77901600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr15:77897000-77901000	Enhancers	Right Atrium	heart
8	chr15:77897200-77900200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
9	chr15:77897200-77901800	Enhancers	K562	blood
10	chr15:77897200-77903000	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr15:77897400-77900200	Enhancers	Rectal Mucosa Donor 29	rectum
12	chr15:77897400-77900800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr15:77897400-77901000	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr15:77897400-77901400	Enhancers	Brain Angular Gyrus	brain
15	chr15:77897400-77901400	Enhancers	Brain Cingulate Gyrus	brain
16	chr15:77897400-77901400	Enhancers	Brain Hippocampus Middle	brain
17	chr15:77897400-77901600	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr15:77897400-77903800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr15:77897600-77900400	Enhancers	Right Ventricle	heart
20	chr15:77897600-77901800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr15:77897800-77901800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr15:77898000-77903800	Weak transcription	Fetal Brain Female	brain
23	chr15:77898200-77900200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
24	chr15:77898200-77900600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr15:77898200-77901400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr15:77898200-77902000	Enhancers	Placenta	Placenta
27	chr15:77898400-77900200	Weak transcription	Brain Germinal Matrix	brain
28	chr15:77898400-77906400	Weak transcription	Pancreas	Pancrea
29	chr15:77898600-77900800	Enhancers	Fetal Stomach	stomach
30	chr15:77898600-77902200	Enhancers	Brain Substantia Nigra	brain
31	chr15:77898600-77903200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr15:77898800-77900200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr15:77898800-77900400	Enhancers	Left Ventricle	heart
34	chr15:77898800-77900600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr15:77898800-77900800	Enhancers	NHDF-Ad	bronchial
36	chr15:77898800-77901000	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr15:77899000-77900200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr15:77899000-77900200	Enhancers	Fetal Intestine Small	intestine
39	chr15:77899000-77901000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
40	chr15:77899200-77900200	Enhancers	HSMMtube	muscle
41	chr15:77899200-77900400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr15:77899200-77901400	Enhancers	Brain Anterior Caudate	brain
43	chr15:77899200-77903800	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr15:77899200-77905800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr15:77899400-77901600	Weak transcription	Colonic Mucosa	Colon
46	chr15:77899400-77902000	Weak transcription	Fetal Kidney	kidney
47	chr15:77899400-77904200	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr15:77899600-77903400	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr15:77899800-77901000	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr15:77899800-77901200	Enhancers	GM12878-XiMat	blood

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